Enhanced Herbal Smoking Blend

ABSTRACT

The disclosed embodiments relate generally to herbal smoking blends and methods for preparing and using herbal smoking blends. Some embodiments relate to a method of preparing an herbal smoking blend, comprising providing a smoking herb preparation comprising  cannabis , providing a terpenoid solution comprising at least one terpenoid, providing one or more mercaptans or one or more flavonoids, and adding the terpenoid solution and adding the one or more mercaptans or the one or more flavonoids to the smoking herb preparation. Other embodiments are also included within the scope of the invention.

CROSS-REFERENCE TO RELATED APPLICATIONS

This U.S. national stage patent application is based off PCT/US2021/029797 which was filed Apr. 29, 2021, which in turn claims priority to U.S. provisional patent application Ser. No. 63/167,933 filed Mar. 30, 2021.

FIELD OF THE INVENTION

The disclosed embodiments relate generally to herbal smoking blends and methods for preparing and using herbal smoking blends. Some embodiments relate to a method of preparing an herbal smoking blend, comprising providing a smoking herb preparation comprising cannabis, providing a terpenoid solution comprising at least one terpenoid, providing one or more mercaptans or one or more flavonoids, and adding the terpenoid solution and adding the one or more mercaptans or the one or more flavonoids to the smoking herb preparation. Other embodiments are also included within the scope of the invention.

BACKGROUND

The smoking of various herbs can provide physiological and/or psychological effects, some of which can provide therapeutic benefits. For example, cannabis, also known as marijuana, is an herb that can be smoked for recreational purposes or therapeutic purposes, such as to treat nausea, pain, muscle spasticity, and loss of appetite, among other conditions. It has been observed that different herbs, including different species, different strains, or different varieties of an herb can have different therapeutic effects. Consequently, different species, strains, or varieties of herbs have been cultivated to achieve desired effects. Such cultivation, however, can be time-consuming, can limit the availability of herbs with a desired effect, and may be cost-prohibitive for rare or difficult to cultivate plants.

Accordingly, there is a continuing need for methods of providing smoking herbs with desired effects.

SUMMARY OF PREFERRED EMBODIMENTS

In one representative embodiment of the present invention, a method of preparing an herbal smoking blend comprises providing a smoking herb preparation comprising cannabis, providing a terpenoid solution comprising at least one terpenoid, providing one or more mercaptans, and adding the terpenoid solution and adding the one or more mercaptans to the smoking herb preparation. In another embodiment, the terpenoid is not naturally occurring in the herb preparation. In another embodiment, the terpenoid is selected from the group consisting of pulegone, terpineol-4-ol, p-cymene, borneol, eugenol, sabinene, linalyl acetate, chamazulene, beta-farnesene, benzyl benzoate, benzyl acetate, geraniol, geranyl acetate and combinations thereof. In another embodiment, the terpenoid solution comprises an essential oil mixture. In yet another embodiment, the essential oil mixture comprises at least one essential oil extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, Citrus Limonum or a combination thereof. In yet another embodiment, the essential oil mixture comprises first and second essential oils extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, or Citrus Limonum, and wherein a volume ratio between first and second essential oils is between about 0.01:1 and about 1:1. In yet another embodiment, the terpenoid solution further comprises a solvent, wherein the solvent comprises ethanol and water. In yet another embodiment, the terpenoid solution comprises about 1% to about 5% by volume of the essential oil mixture, about 40% to about 90% by volume of ethanol and about 10% to about 30% by volume of water. In yet another embodiment, the smoking herb preparation comprises at least one phytocannabinoid selected from the group consisting of delta-9-tetrahydrocannabinol (THC), cannabidiol (CBD), cannabichromene (CBC), cannabigerol (CBG), tetrandrocannabivarin (THCV), cannabidivarin (SBDV) and cannabinol (CBN). In yet another embodiment, the smoking herb preparation comprises any type of cannabinoid or any combination of cannabinoids. In yet another embodiment, the smoking herb preparation comprises a smoking herb other than cannabis. In yet another embodiment, the terpenoid is derived from a plant other than cannabis. In yet another embodiment, adding the terpenoid solution comprises applying the terpenoid solution in a liquid state to the smoking herb preparation, and adding the one or more mercaptans comprises applying the one or more mercaptans in a liquid state to the smoking herb preparation. In yet another embodiment, adding the terpenoid solution comprises dropping droplets of the terpenoid solution onto the smoking herb preparation, and adding the one or more mercaptans comprises dropping droplets of the one or more mercaptans onto the smoking herb preparation. In yet another embodiment, adding the terpenoid solution comprises at least partially immersing the smoking herb into the terpenoid solution. In yet another embodiment, the smoking herb preparation comprises a smoking herb rolled in a rolling paper, and wherein adding the terpenoid comprises impregnating the rolling paper with the terpenoid solution. In yet another embodiment, the smoking herb preparation comprises a smoking herb and a rolling sheet, and wherein the method further comprises rolling the smoking herb into a cylinder to at least partially confine the smoking herb. In yet another embodiment, an amount of the at least one terpenoid added to the smoking herb preparation exceeds a naturally existing amount of cannabis terpenoid in the smoking herb by about 10% to about 1000%. In yet another embodiment, the one or more mercaptans are selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan and combinations thereof.

In another representative embodiment of the present invention, a smoking herb preparation system comprises a smoking herb comprising cannabis; a terpenoid solution comprising at least one terpenoid; one or more mercaptans; and an applicator for administering a dose of the terpenoid solution and the one or more mercaptans, and combinations thereof, to the smoking herb. In yet another embodiment, the terpenoid is not naturally occurring in the herb preparation. In yet another embodiment, the at least one terpenoid selected from the group consisting of pulegone, terpineol-4-ol, p-cymene, borneol, eugenol, sabinene, linalyl acetate, chamazulene, beta-farnesene, benzyl benzoate, benzyl acetate, geraniol, geranyl acetate and combinations thereof. In yet another embodiment, the terpenoid solution comprises an essential oil mixture. In yet another embodiment, the essential oil mixture comprises at least one essential oil extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, Citrus Limonum, and combinations thereof. In yet another embodiment, the terpenoid solution further comprises a solvent including ethanol and water. In yet another embodiment, the applicator comprises a dropper. In yet another embodiment, the applicator comprises a sprayer. In yet another embodiment, the one or more mercaptans are selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan and combinations thereof.

In another representative embodiment of the present invention, an herbal smoking blend comprises a smoking herb comprising cannabis; a terpenoid incorporated in the smoking herb at a terpenoid concentration, wherein the terpenoid is not naturally occurring in the smoking herb at the terpenoid concentration; and one or more mercaptans. In yet another embodiment, the herbal smoking blend comprises at least one essential oil extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, Citrus Limonum, and combinations thereof. In yet another embodiment, the terpenoid is not naturally occurring in the smoking herb. In yet another embodiment, the terpenoid is selected from the group consisting of pulegone, terpineol-4-ol, p-cymene, borneol, eugenol, sabinene, linalyl acetate, chamazulene, beta-farnesene, benzyl benzoate, benzyl acetate, geraniol, geranyl acetate and combinations thereof. In yet another embodiment, the one or more mercaptans are selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan and combinations thereof.

In another representative embodiment of the present invention, a smoking herb preparation system, comprises a smoking herb comprising cannabis; a terpenoid solution comprising a terpenoid selected from the group consisting of 1,8-cineole, d-limonene, α-terpineol and combinations thereof; one or more mercaptans selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan and combinations thereof; and an applicator for administering a dose of the terpenoid solution and the one or more mercaptans, and combinations thereof, to the smoking herb.

Additional representative embodiments of the present invention are discussed in more detail herein. It is to be understood that these representative embodiments do not limit the scope of the present invention in any way. The representative embodiments described herein are provided as examples to illustrate the broad scope of the present invention.

BRIEF DESCRIPTION OF THE FIGURES

These and other aspects and advantages of the invention will become apparent and more readily appreciated from the following description, taken in conjunction with the accompanying figures.

FIG. 1 is a flow chart illustrating a method of preparing an herbal smoking blend, according to some embodiments.

FIG. 2 is a schematic illustration of a smoking herb preparation system comprising a smoking herb, according to some embodiments.

FIG. 3 is a schematic illustration of a smoking herb preparation system comprising a smoking herb, according to some other embodiments.

FIG. 4 is a schematic illustration of a smoking herb preparation system comprising a smoking herb, according to yet other embodiments.

These figures illustrate certain non-limiting embodiments of the present invention. These non-limiting embodiments do not limit the scope of the present invention in any way.

DESCRIPTION OF PREFERRED EMBODIMENTS

Although the detailed description herein contains many details for the purposes of illustration, it is to be understood that there is no intent to limit the scope to the embodiments disclosed herein. On the contrary, the intent is to cover all alternatives, modifications, and equivalents within the broad scope of the present invention.

Since the discovery of therapeutic effects of inhaled smoke of cannabis, the chemical origins of the therapeutic effects have been an intense area of research. The primary focus of the research into the chemical origins of the therapeutic effects of cannabis has been centered around a class of active compounds called cannabis phytocannabinoids. Phytocannabinoids, also referred to as cannabinoids, refer to a group of C₂₁ terpenophenolic compounds that are uniquely produced in cannabis. The most widely known phytocannabinoid is tetrahydrocannabidol (THC), which is known to be responsible for producing psychoactivity commonly associated with cannabis. Since the isolation of THC, other phytocannabinoids have been isolated and some have been associated with therapeutic effects. While over 100 phytocannabinoids are known to exist, a group of well-documented phytocannabinoids include tetrahydrocannabidol (THC), cannabidiol (CBD), cannabichromene (CBC), cannabigerol (CBG), tetrandrocannabivarin (THCV), cannabidivarin (CBDV) and cannabinol (CBN). Some of the therapeutic effects of phytocannabinoids include, without being bound to any theory, euphoric effects (associated, for example, with THC and THCV), analgesic effects (associated, for example, with THC, CBD and THCV), sedative effects (associated, for example, with CBD), antipsychotic effects (associated, for example, with CBD), anti-inflammatory effects (associated, for example, with THC, CBD, CBC, CBG and CBN), anti-convulsant effects (associated, for example, with CBD and CBN), antibiotic effects (associated, for example, with CBC, CBN and CBG), and anti-fungal effects (associated, for example, with CBC and CBG), to name a few. Under certain circumstances, there may be synergistic enhancement of certain therapeutic effects in naturally occurring cannabis when certain amounts and/or ratios of phytocannabinoids are present in combination. For example, an overall enhancement in therapeutic effects of cannabis may be achieved when a certain balance is struck between THC and CBD. For example, sedative effects of CBD may serve to oppose certain undesirable effects of THC, such as anxiety, thereby enhancing the overall therapeutic effects.

Other isolated compounds of cannabis may have certain therapeutic effects when inhaled as part of cannabis smoke, including terpenoids, flavonoids, and phytosterol. Terpenoids are derived from repeating units of isoprene (C₅H₈), such as monoterpenoids (with C₁₀ skeletons), sesquiterpenoids (C₁₅), diterpenoids (C₂₀), and triterpenoids (C₃₀). The final structure of terpenoids can range from simple linear chains to complex molecules and may simply be a hydrocarbon, or may include alcohol, ether, aldehyde, ketone, or ester functional groups attached to a carbon skeleton. As used herein, the term terpenoids include terpenes. Over 200 naturally occurring terpenoids have been identified and isolated from cannabis. Such terpenoids include d-limonene, α-pinene, β-myrcene, linalool, pulegone, 1,8-cineole (eucalyptol), α-terpineol, terpineol-4-ol, p-cymene, borneol, Δ-3-carene, β-caryophyllene, caryophyllene oxide, nerolidol, and phytol. Some of the therapeutic effects of terpenoids include, without being bound to any theory, analgesic effects (associated, for example, with β-myrcene), sedative effects (associated, for example, with linalool, pulegone and α-terpineol), antidepressant effects (associated, for example, with linalool and d-limonene), anti-inflammatory effects (associated, for example, with β-myrcene, β-caryophyllene, 1,8-cineole, α-pinene and Δ-3-carene), anti-mutagenic effects (associated, for example, with β-myrcene and d-limonene), antibiotic effects (associated, for example, with β-myrcene, 1,8-cineole, p-cymene, terpineol-4-ol, borneol and α-pinene), and Acetylcholinesterase (AChE) inhibitor effects (associated, for example, with pulegone, p-cymene, terpineol-4-ol and α-terpineol), to name a few. It will be appreciated that, under certain circumstances, there may be synergistic enhancement of certain therapeutic effects in naturally occurring cannabis when certain amounts and/or ratios of terpenoids are present in combination.

In addition, under certain circumstances, when phytocannabinoids and terpenoids are simultaneously present in cannabis, there may also be cross-compound synergistic effects. That is, the therapeutic effects obtained from cannabis having certain combinations of some phytocannabinoids and some terpenoids is greater than the sum of therapeutic effects obtained from the phytocannabinoids or the terpenoids taken alone. For example, without being bound to any theory, analgesic effects of THC may be synergistically boosted by various terpenoids, anticonvulsant effects of CBD and THCV may be synergistically boosted by linalool, anti-inflammatory/antifungal effects of CBC and CBG may be synergistically boosted by caryophyllene oxide, anti-inflammatory/analgesic effects of CBC may be synergistically boosted by various terpenoids, sedative effects of CBN may be synergistically boosted by β-myrcene and nerolidol, to name just few examples of synergistic effects when phytocannabinoids and terpenoids are inhaled together as part of cannabis smoke.

Naturally occurring therapeutic compounds in cannabis, including phytocannabinoids and terpenoids, are synthesized in secretory cells inside glandular trichomes of cannabis. In addition, different strains of cannabis produce and can be bred to produce varying amounts of certain compounds. For example, common “street” cannabis may have been bred such that relatively high amounts of THC are present to maximize the “high” of the person using the cannabis for recreational purposes. The same strain of “street” cannabis, however, may not have been bred to maximize, and therefore contain less than desired amounts of terpenoids or phytocannabinoids other than THC. As a result, while the effect of such cannabis strain as a euphoriant may be relatively high, their therapeutic effects may be relatively low. Therefore, to improve the therapeutic effects and to target certain therapeutic effects from cannabis, attempts to cultivate different strains of cannabis having particular combinations and amounts of specific phytocannabinoids and terpenoids have been made. However, such effort has been time consuming and not necessarily aimed at mass cultivation to serve the general public.

While some terpenoids naturally occur in cannabis, terpenoids also naturally occur in plants other than cannabis. As with cannabis, terpenoids in some plants give rise to the distinctive odor of the plants. For example, d-limonene occurs naturally in citrus plants, and is the predominant compound that gives rise to the familiar scent of citrus. Similarly, α-pinene occurs naturally in coniferous plants and is the predominant compound that gives rise to the familiar scent of pine. Thus, some terpenoids, such as d-limonene and α-pinene, occur relatively abundantly.

It has been found that the therapeutic effects of smoking herbs may be tailored by varying the terpenoid composition of the smoking herbs. In some embodiments the smoking herb may be cannabis and the therapeutic effects may include synergistic effects between the phytocannabinoids that are naturally present in a particular strain of cannabis and terpenoids that may be isolated from plants other than the particular strain of cannabis or other than cannabis in general. The terpenoids may be added to a preparation made from the particular strain of cannabis and may provide a terpenoid concentration that is just as high, if not higher, than terpenoid levels that are naturally occurring in, for example, other cannabis strains. Thus, in some embodiments, the terpenoid added to the smoking herb preparation may be at a higher concentration than that naturally found in the smoking herb or the terpenoid may not be naturally produced by the smoking herb plant at all.

It will be appreciated that adding desired types and amounts of terpenoids from plants other than the particular strain cannabis can offer several advantages. For example, terpenoids from other plants can be economically favorable compared to, for example, breeding particular strains of cannabis having similar types and amounts of terpenoids. In addition, the desired types and amounts can be targeted more specifically to enhance or magnify known therapeutic effects, or even create new therapeutic effects that may not be possible using natural or engineered strains of cannabis alone.

Other Representative Embodiments: Addition of One or More Thiols or Mercaptans

The present invention also contemplates that one or more thiols or mercaptans described herein can be mixed with a terpenoid solution to provide desired properties including but not limited to desired odor or fragrance and/or flavor, for example, as fragrance agents and/or flavoring agents. The mixture of one or more thiols or mercaptans with a terpenoid solution, as described herein, can also produce unexpected, beneficial and positive synergistic effects including enhanced aromas and an overall enhanced sensory experience for a user. In addition, there may also be synergistic enhancement of certain therapeutic effects in naturally occurring cannabis when certain amounts and/or ratios of terpenoids are present in combination with one or more thiols or mercaptans.

As used herein, it is to be understood that the terms “thiol” and “mercaptan” can be used interchangeably and they include organosulfur compounds that contain a sulfur-hydrogen bond. A mercapto group or thiol group is a functional group that contains a sulfur atom bonded to a hydrogen atom (or “—SH” functional group). Therefore it is to be understood that thiols, which may also be referred to herein as mercaptans, can include any organosulfur compound of the form R—SH, in which R represents an alkyl substituent or other organic substituent.

One or more of the thiols or mercaptans described herein can have a sulfurous odor. Other thiols or mercaptans provide other stinky cannabis aromas. When mixed with terpenoids as described herein, the one or more mercaptans can provide other desired aromas.

In certain embodiments, one or more mercaptans can be used, for example, in combination or mixture with one or more terpenes. As described herein, representative examples of one or more mercaptans that can be used in accordance with the present invention include but are not limited to mercaptans that are selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan and combinations thereof.

As described elsewhere herein, a terpenoid solution can be mixed with one or more thiols or mercaptans. It is preferred that a terpenoid solution can be mixed with any amount, percentage or ratio of one or more thiols or mercaptans, as determined and measured for example on a volume by volume basis, a weight by volume basis or a weight by weight basis.

In other embodiments, one or more thiols or mercaptans can be used, for example, in combination or mixture with one or more terpenes and essential oils. In certain embodiments, a terpenoid solution can thus be mixed with one or more mercaptans as described herein in addition to an essential oil mixture. As described elsewhere herein, a terpenoid solution can be mixed with any amount, percentage or ratio of one or more mercaptans, as determined and measured for example on a volume by volume basis, a weight by volume basis or a weight by weight basis.

The one or more thiols or mercaptans can preferably be used in liquid form. Preferably, the one or more thiols or mercaptans, for use as described herein, can be prepared as a solution by diluting the thiols or mercaptans in one or more suitable solvents. In certain embodiments, any of the thiols or mercaptans described herein can be diluted to any extent, as needed or desired, in one or more appropriate or suitable solvents, for example, on a volume by volume basis or other basis. In a preferred embodiment, prenyl mercaptan or another mercaptan can be diluted in a suitable solvent before mixing with a terpenoid solution. According to one example, a stock concentration of prenyl mercaptan (e.g., from a supplier) can be diluted and prepared as a 10:90 prenyl mercaptan:ethanol solution, i.e., a solution that contains 10 percent prenyl mercaptan by volume and 90 percent ethanol by volume, on a volume by volume basis. The 10:90 prenyl mercaptan:ethanol solution can then be mixed with a terpenoid solution.

In certain embodiments, the one or more thiols or mercaptans described herein can be dissolved in one or more solvents that are safe if ingested, inhaled or consumed by a human in an amount that is determined by advance testing to be safe to humans.

As described herein, one or more mercaptans described herein can preferably provide additional desired odor or fragrance and/or flavor, for example, as fragrance agents and/or flavoring agents. One or more of the thiols or mercaptans described herein can have a sulfurous odor. Other thiols or mercaptans provide other stinky cannabis aromas. When mixed with terpenoids as described herein, the one or more mercaptans can provide other desired aromas.

In other embodiments, the one or more thiols or mercaptans described herein can also be mixed with one or more solubilizing agents that are safe if ingested, inhaled or consumed by a human in an amount that is determined by advance testing to be safe to humans.

In yet other embodiments, the one or more thiols or mercaptans described herein can also be mixed with one or more other types of excipients that are safe if ingested, inhaled or consumed by a human in an amount that is determined by advance testing to be safe to humans.

Other Representative Embodiments

As described elsewhere herein, the present invention contemplates various other representative embodiments as described in further detail below.

In one embodiment, the present invention contemplates a method of preparing an herbal smoking blend, comprising: providing a smoking herb preparation comprising cannabis; providing (i) a terpenoid solution comprising at least one terpenoid; providing (ii) one or more mercaptans; and (iii) adding the terpenoid solution and adding the one or more mercaptans to the smoking herb preparation. In another embodiment, the present invention further contemplates wherein the one or more mercaptans is selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan, or any combination thereof.

In another embodiment, the present invention contemplates a method of preparing an herbal smoking blend, comprising: providing a smoking herb preparation comprising cannabis; providing (i) a terpenoid solution comprising at least one terpenoid; providing (ii) one or more flavonoids; and (iii) adding the terpenoid solution and adding the one or more flavonoids to the smoking herb preparation. In another embodiment, the present invention further contemplates wherein the one or more flavonoids include, but are not limited to, any anthoxanthin (flavone and flavonol), bioflavonoid, isoflavonoid, neoflavonoid, prenylated flavonoids or prenylflavonoids, prenylated isoflavonoids or any combination thereof. In still yet another embodiment, the present invention further contemplates wherein the prenylated flavonoids or prenylflavonoids include, but are not limited to, cannflavins including, but not limited to, cannflavin A (CFL-A), B (CFL-B) and C (CFL-C), isocannflavin B (IsoB), or any combination thereof. In still yet another embodiment, the prenylflavonoids include, but are not limited to, 6-geranylnaringenin, isoxanthohumol, 8-Prenylkaempferol, 6-Prenylnaringenin, epimedin C, 8-prenylnaringenin, 6,8-Diprenyleriodictyol, Australone A, dorsmanin C and dorsmanin F, or any combination thereof. In still yet another embodiment, the present invention further contemplates that any flavonoid can be prepared in a suitable solvent, or one or more solvents, and a flavonoid solution for example can thus be obtained.

In yet another embodiment, the present invention contemplates a method of preparing an herbal smoking blend, comprising: providing a smoking herb preparation comprising cannabis; providing (i) a terpenoid solution comprising at least one terpenoid; also providing (ii) one or more mercaptans or one or more flavonoids; and (iii) adding the terpenoid solution and adding the one or more mercaptans or the one or more flavonoids to the smoking herb preparation. In another embodiment, the present invention further contemplates wherein the one or more mercaptans is selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan, or any combination thereof. In another embodiment, the present invention further contemplates wherein the one or more flavonoids include, but are not limited to, any anthoxanthin (flavone and flavonol), bioflavonoid, isoflavonoid, neoflavonoid, prenylated flavonoids or prenylflavonoids, prenylated isoflavonoids or any combination thereof. In still yet another embodiment, the present invention further contemplates wherein the prenylated flavonoids or prenylflavonoids include, but are not limited to, cannflavins including, but not limited to, cannflavin A (CFL-A), B (CFL-B) and C (CFL-C), isocannflavin B (IsoB), or any combination thereof. In still yet another embodiment, the prenylflavonoids include, but are not limited to, 6-geranylnaringenin, isoxanthohumol, 8-Prenylkaempferol, 6-Prenylnaringenin, epimedin C, 8-prenylnaringenin, 6,8-Diprenyleriodictyol, Australone A, dorsmanin C and dorsmanin F, or any combination thereof. In still yet another embodiment, the present invention further contemplates that any flavonoid can be prepared in a suitable solvent, or one or more solvents, and a flavonoid solution for example can thus be obtained.

In yet another embodiment, the present invention contemplates a method of preparing an herbal smoking blend, comprising: providing a smoking herb preparation comprising cannabis; providing (i) a terpenoid solution comprising at least one terpenoid; also providing (ii) one or more mercaptans and one or more flavonoids; and (iii) adding the terpenoid solution and adding the one or more mercaptans and the one or more flavonoids to the smoking herb preparation. In another embodiment, the present invention further contemplates wherein the one or more mercaptans is selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan, or any combination thereof. In another embodiment, the present invention further contemplates wherein the one or more flavonoids include, but are not limited to, any anthoxanthin (flavone and flavonol), bioflavonoid, isoflavonoid, neoflavonoid, prenylated flavonoids or prenylflavonoids, prenylated isoflavonoids or any combination thereof. In still yet another embodiment, the present invention further contemplates wherein the prenylated flavonoids or prenylflavonoids include, but are not limited to, cannflavins including, but not limited to, cannflavin A (CFL-A), B (CFL-B) and C (CFL-C), isocannflavin B (IsoB), or any combination thereof. In still yet another embodiment, the prenylflavonoids include, but are not limited to, 6-geranylnaringenin, isoxanthohumol, 8-Prenylkaempferol, 6-Prenylnaringenin, epimedin C, 8-prenylnaringenin, 6,8-Diprenyleriodictyol, Australone A, dorsmanin C and dorsmanin F, or any combination thereof. In still yet another embodiment, the present invention further contemplates that any flavonoid can be prepared in a suitable solvent, or one or more solvents, and a flavonoid solution for example can thus be obtained.

In another representative embodiment, the present invention contemplates a method of preparing an herbal smoking blend, comprising: providing a smoking herb preparation comprising cannabis; providing a terpenoid solution comprising at least one terpenoid; and mixing (i) one or more flavonoids or (ii) one or more mercaptans or thiols with the at least one terpenoid.

In yet another representative embodiment, the present invention contemplates a method of preparing an herbal smoking blend, comprising the following: providing a smoking herb preparation comprising cannabis; providing a terpenoid solution comprising at least one terpenoid, providing one or more mercaptans, providing one or more flavonoids, and adding the terpenoid solution, adding the one or more mercaptans, and adding the one or more flavonoids to the smoking herb preparation.

In another representative embodiment, the present invention contemplates an herbal smoking blend, comprising a smoking herb comprising cannabis, and a terpenoid incorporated in the smoking herb at a terpenoid concentration, wherein the terpenoid is not naturally occurring in the smoking herb at the terpenoid concentration, also comprising one or more mercaptans or one or more flavonoids.

In another representative embodiment, the present invention contemplates an herbal smoking blend, comprising a smoking herb comprising cannabis, and a terpenoid incorporated in the smoking herb at a terpenoid concentration, wherein the terpenoid is not naturally occurring in the smoking herb at the terpenoid concentration, also comprising one or more mercaptans and one or more flavonoids.

These are all non-limiting embodiments described herein, for illustration purposes only, and are not intended to limit the scope of the present invention in any way.

The mixture of one or more thiols or mercaptans and one or more flavonoids with a terpenoid solution, as described herein, can also produce unexpected, beneficial and positive synergistic effects including enhanced aromas and an overall enhanced sensory experience for a user. In addition, there may also be synergistic enhancement of certain therapeutic effects in naturally occurring cannabis when certain amounts and/or ratios of terpenoids are present in combination with one or more thiols or mercaptans and one or more flavonoids.

As described elsewhere herein, the term terpenoids is intended to include terpenes. In a preferred embodiment, the present invention contemplates that additives to terpenes can include different groups including, for example, one or more thiols/mercaptans, one or more flavonoids, one or more cannabinoids, or any combination of two of the aforementioned groups or three of the aforementioned groups.

As described herein, the present invention also contemplates that the term “cannabinoid” as used herein is intended to include any type of cannabinoid, and the term “cannabinoids” can include any combination of different types of cannabinoids. Moreover, the term “phytocannabinoid” is intended to include any type of phytocannabinoid, and the term “phytocannabinoids” can include any combination of different types of phytocannabinoids.

The present invention also contemplates a method of preparing an herbal smoking blend, comprising: providing a smoking herb preparation comprising cannabis; providing a terpenoid solution comprising at least one terpenoid; providing one or more mercaptans or one or more flavonoids; and adding the terpenoid solution and adding the one or more mercaptans or the one or more flavonoids to the smoking herb preparation.

Other Representative Embodiments

The present invention also contemplates other preferred embodiments as described herein. In one representative embodiment of the present invention, a method of preparing an herbal smoking blend comprises providing a smoking herb preparation comprising cannabis, providing a terpenoid solution comprising at least one terpenoid, providing one or more mercaptans, and adding the terpenoid solution and adding the one or more mercaptans to the smoking herb preparation. In another embodiment, the terpenoid is not naturally occurring in the herb preparation. In another embodiment, the terpenoid is selected from the group consisting of pulegone, terpineol-4-ol, p-cymene, borneol, eugenol, sabinene, linalyl acetate, chamazulene, beta-farnesene, benzyl benzoate, benzyl acetate, geraniol, geranyl acetate and combinations thereof. In another embodiment, the terpenoid solution comprises an essential oil mixture. In yet another embodiment, the essential oil mixture comprises at least one essential oil extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, Citrus Limonum or a combination thereof. In yet another embodiment, the essential oil mixture comprises first and second essential oils extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, or Citrus Limonum, and wherein a volume ratio between first and second essential oils is between about 0.01:1 and about 1:1. In yet another embodiment, the terpenoid solution further comprises a solvent, wherein the solvent comprises ethanol and water. In yet another embodiment, the terpenoid solution comprises about 1% to about 5% by volume of the essential oil mixture, about 40% to about 90% by volume of ethanol and about 10% to about 30% by volume of water. In yet another embodiment, the smoking herb preparation comprises at least one phytocannabinoid selected from the group consisting of delta-9-tetrahydrocannabinol (THC), cannabidiol (CBD), cannabichromene (CBC), cannabigerol (CBG), tetrandrocannabivarin (THCV), cannabidivarin (SBDV) and cannabinol (CBN). In yet another embodiment, the smoking herb preparation comprises any type of cannabinoid. In yet another embodiment, the smoking herb preparation comprises a smoking herb other than cannabis. In yet another embodiment, the terpenoid is derived from a plant other than cannabis. In yet another embodiment, adding the terpenoid solution comprises applying the terpenoid solution in a liquid state to the smoking herb preparation, and adding the one or more mercaptans comprises applying the one or more mercaptans in a liquid state to the smoking herb preparation. In yet another embodiment, adding the terpenoid solution comprises dropping droplets of the terpenoid solution onto the smoking herb preparation, and adding the one or more mercaptans comprises dropping droplets of the one or more mercaptans onto the smoking herb preparation. In yet another embodiment, adding the terpenoid solution comprises at least partially immersing the smoking herb into the terpenoid solution. In yet another embodiment, the smoking herb preparation comprises a smoking herb rolled in a rolling paper, and wherein adding the terpenoid comprises impregnating the rolling paper with the terpenoid solution. In yet another embodiment, the smoking herb preparation comprises a smoking herb and a rolling sheet, and wherein the method further comprises rolling the smoking herb into a cylinder to at least partially confine the smoking herb. In yet another embodiment, an amount of the at least one terpenoid added to the smoking herb preparation exceeds a naturally existing amount of cannabis terpenoid in the smoking herb by about 10% to about 1000%. In yet another embodiment, the one or more mercaptans are selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan and combinations thereof.

In another representative embodiment of the present invention, a smoking herb preparation system comprises a smoking herb comprising cannabis; a terpenoid solution comprising at least one terpenoid; one or more mercaptans; and an applicator for administering a dose of the terpenoid solution and the one or more mercaptans, and combinations thereof, to the smoking herb. In yet another embodiment, the terpenoid is not naturally occurring in the herb preparation. In yet another embodiment, the at least one terpenoid selected from the group consisting of pulegone, terpineol-4-ol, p-cymene, borneol, eugenol, sabinene, linalyl acetate, chamazulene, beta-farnesene, benzyl benzoate, benzyl acetate, geraniol, geranyl acetate and combinations thereof. In yet another embodiment, the terpenoid solution comprises an essential oil mixture. In yet another embodiment, the essential oil mixture comprises at least one essential oil extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, Citrus Limonum, and combinations thereof. In yet another embodiment, the terpenoid solution further comprises a solvent including ethanol and water. In yet another embodiment, the applicator comprises a dropper. In yet another embodiment, the applicator comprises a sprayer. In yet another embodiment, the one or more mercaptans are selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan and combinations thereof.

In another representative embodiment of the present invention, an herbal smoking blend comprises a smoking herb comprising cannabis; a terpenoid incorporated in the smoking herb at a terpenoid concentration, wherein the terpenoid is not naturally occurring in the smoking herb at the terpenoid concentration; and one or more mercaptans. In yet another embodiment, the herbal smoking blend comprises at least one essential oil extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, Citrus Limonum, and combinations thereof. In yet another embodiment, the terpenoid is not naturally occurring in the smoking herb. In yet another embodiment, the terpenoid is selected from the group consisting of pulegone, terpineol-4-ol, p-cymene, borneol, eugenol, sabinene, linalyl acetate, chamazulene, beta-farnesene, benzyl benzoate, benzyl acetate, geraniol, geranyl acetate and combinations thereof. In yet another embodiment, the one or more mercaptans are selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan and combinations thereof.

In another representative embodiment of the present invention, a smoking herb preparation system, comprises a smoking herb comprising cannabis; a terpenoid solution comprising a terpenoid selected from the group consisting of 1,8-cineole, d-limonene, α-terpineol and combinations thereof; one or more mercaptans selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan and combinations thereof; and an applicator for administering a dose of the terpenoid solution and the one or more mercaptans, and combinations thereof, to the smoking herb.

Reference will now be made to the drawings, in which like numerals refer to like parts throughout.

FIG. 1 is a flow chart illustrating a method 10 of preparing an herbal smoking blend, according to some embodiments. The method of preparing an herbal smoking blend comprises providing a smoking herb preparation (step 20, as shown in FIG. 1 ). The method additionally includes providing a terpenoid solution comprising a terpenoid (step 30, as shown in FIG. 1 ). The method further includes providing one or more mercaptans or one or more flavonoids, or combinations thereof, as described herein (step 35, as shown in FIG. 1 ). The method further includes adding the terpenoid solution and the one or more mercaptans or one or more flavonoids to the smoking herb preparation (step 40, as shown in FIG. 1 ).

In some embodiments, providing the smoking herb preparation (step 20) includes providing a smoking herb including smoking cannabis, including any species, subspecies, strain or variety of cannabis. The herb preparation can include any part of the plant of the cannabis, including the leaf, the root, the stem, the flower, or any other part of the plant that occurs naturally. In some embodiments, the smoking herb includes cannabis plants cultivated for fiber and seed production, sometimes described as low-intoxicant, non-drug, or fiber types. In some other embodiments, the smoking herb includes cannabis plants cultivated for drug production, sometimes described as high-intoxicant or drug types. In some other embodiments, the smoking herb includes cannabis plants that are escaped, hybridized, or wild forms of either of the above types.

In some embodiments, a preparation includes smoking herb that has been sufficiently dried so that it can be combusted under ordinary ambient conditions, such that the resulting smoke can be inhaled. In some embodiments, a preparation includes a smoking herb and a rolling paper that can be used to roll the smoking herb into a thin cylinder using a rolling paper, similar to a cigarette.

In other embodiments, referring again to FIG. 1 , providing the smoking herb preparation (step 20) can include providing a smoking herb other than cannabis. Examples of other smoking herbs include Amaranthus dubius, Arctostaphylos uva-ursi, Argemone mexicana, Arnica, Artemisia vulgaris, Calea zacatechichi, Canavalia maritima, Cecropia mexicana, Cestrum nocturnum, Cynoglossum virginianum, Cytisus scoparius, Entada rheedii, Eschscholzia californica, Fittonia albivenis, Hippobroma longiflora, Humulus japonica, Humulus lupulus, Lactuca virosa, Laggera alata, Leonotis leonurus, Leonurus cardiaca, Leonurus sibiricus, Lobelia cardinalis, Lobelia inflata, Lobelia siphilitica, Nepeta cataria, Nicotiana (i.e., tobacco), Nymphaea alba, Opium poppy, Passiflora incarnata, Pedicularis densiflora, Pedicularis groenlandica, Salvia divinorum, Salvia dorrii, Salvia, Scutellaria galericulata, Scutellaria lateriflora, Scutellaria nana, Scutellaria, Sida acuta, Sida rhombifolia, Silene capensis, Syzygium aromaticum, Tagetes lucida, Tarchonanthus camphoratus, Turnera diffusa, Verbascum, and Zornia latifolia, to name a few.

In some embodiments, providing the smoking herb preparation (step 20) comprises providing a smoking herb comprising at least one phytocannabinoid, such as a phytocannabinoid selected from the group consisting of delta-9-tetrahydrocannabinol (THC), cannabidiol (CBD), cannabichromene (CBC), cannabigerol (CBG), tetrahydrocannabivarin (THCV), cannabidivarin (SBDV) and cannabinol (CBN). In another embodiment, providing the smoking herb preparation comprises providing a smoking herb comprising any type of cannabinoid or any combination of cannabinoids.

The present invention contemplates that the term “cannabinoid” as used herein is intended to include any type of cannabinoid, and the term “cannabinoids” can include any combination of different types of cannabinoids. Moreover, the term “phytocannabinoid” is intended to include any type of phytocannabinoid, and the term “phytocannabinoids” can include any combination of different types of phytocannabinoids.

In some embodiments, providing the smoking herb preparation (step 20) comprises providing a smoking herb other than cannabis. In some embodiments, for example where a synergistic effect between a phytocannabinoid and terpenoids is desired, the smoking herb other than cannabis may comprise at least one added phytocannabinoid, such as a phytocannabinoid selected from the group consisting of delta-9-tetrahydrocannabinol (THC), cannabidiol (CBD), cannabichromene (CBC), cannabigerol (CBG), tetrandrocannabivarin (THCV), cannabidivarin (SBDV) and cannabinol (CBN).

Still referring to FIG. 1 the illustrated method of method 10 of preparing an herbal smoking blend additionally includes providing a terpenoid solution (step 30) comprising a terpenoid. As used herein, a terpenoid solution refers in a preferred embodiment to a mixture comprising at least one terpenoid and a solvent, where at least a portion of the terpenoid is incorporated in the mixture to form the terpenoid solution. The terpenoid can be miscible, immiscible, or partially miscible in the solvent. In embodiments where the terpenoid is at least partially immiscible, the resulting mixture is sometimes referred to as an emulsion.

In some embodiments, providing the terpenoid solution (step 30) includes providing a solution including a terpenoid selected from the group consisting of d-limonene, α-pinene, β-myrcene, linalool, pulegone, 1,8-cineole (eucalyptol), α-terpineol, terpineol-4-ol, p-cymene, borneol, Δ-3-carene, β-caryophyllene, caryophyllene oxide, nerolidol, phytol, Eugenol, Sabinene, Linalyl Acetate, Camphor, Chamazulene, beta-Farnesene, alpha-Humulene, Benzyl Benzoate, Benzyl Acetate, Geraniol, Geranyl Acetate, gamma-Terpinene, beta-Pinene, and combinations thereof.

In some embodiments, providing the terpenoid solution (step 30) comprises providing a terpenoid and a solvent, and mixing the terpenoid and the solvent. The solvent can include any liquid, e.g., a volatile liquid, which can incorporate a desired amount of the terpenoid in the terpenoid solution. As used herein, a liquid that incorporates the terpenoid includes a liquid that can hold the terpenoid in either dissolved form or undissolved form (e.g., suspended in the form of an emulsion). In some embodiments, a terpenoid solution having a terpenoid incorporated therein can be a solution having at least 0.1% terpenoid by volume at room temperature and atmospheric pressure.

In some embodiments, the solvent comprises an alcohol, e.g., ethanol, and water. In some embodiments, the terpenoid solution comprises about 1% to about 5% by volume of the terpenoid, about 40% to about 90% by volume of ethanol and about 10% to about 55% by volume of water. In some embodiments, the terpenoid solution comprises about 2% to about 4% by volume of the terpenoid, about 66% to about 80% by volume of ethanol and about 20% to about 30% by volume of water. Advantageously, such a solution can allow the terpenoid to be evenly distributed or suspended in the solvent, thereby facilitating the formation of a homogenous solution that allows a desired quantity of terpenoid to be added to a smoking herb preparation.

Still referring to FIG. 1 , in some embodiments, the terpenoid in the terpenoid solution can be in a substantially purified form including a targeted terpenoid selected from the group consisting of d-limonene, α-pinene, β-myrcene, linalool, pulegone, 1,8-cineole (eucalyptol), α-terpineol, terpineol-4-ol, p-cymene, borneol, Δ-3-carene, β-caryophyllene, caryophyllene oxide, nerolidol, phytol, and combinations thereof. As used herein, a substantially purified terpenoid refers to the terpenoid being free of impurities other than the targeted terpenoids, with a volume percent of the impurities not exceeding about 5%, about 1%, or about 0.1%. For example, if a substantially pure terpenoid includes a first terpenoid (e.g., d-limonene) and a second terpenoid (e.g. α-pinene) as targeted terpenoids, any other substance including other terpenoids (e.g., β-myrcene, linalool, etc.) would be considered impurities.

As described above, terpenoids can naturally originate from cannabis or other plants. In some embodiments, the terpenoid in the terpenoid solution does not naturally occur in the herb or herbs forming the smoking herb preparation. In some embodiments where the smoking herb preparation includes cannabis, providing the terpenoid solution (step 30) includes providing a solution including a terpenoid that is derived from a plant other than cannabis in general. In some other embodiments where the smoking herb preparation includes cannabis, providing the terpenoid solution (step 30) includes providing a solution including a terpenoid that is derived from a plant other than the cannabis strain from which the smoking herb has been prepared.

In some embodiments, the terpenoid in the terpenoid solution can be provided in the form of an essential oil. An essential oil, sometimes referred to as a volatile oil, an ethereal oil, or an athereola, refers to a concentrated liquid extracted from a plant that can contain, among other compounds, terpenoids. Compounds such as terpenoids included in essential oil often carry a distinctive scent, or essence (hence the name).

In some embodiments, the essential oils can be prepared using one of several methods including, without limitation, distillation, expression and solvent extraction, among others. In distillation, raw plant material, which can include the flowers, leaves, wood, bark, roots, seeds, and/or peel, is put into a distillation apparatus over water. The water is then heated above the boiling point to generate steam therefrom, which passes through the plant material. As the stem passes through the plant material, the volatile compounds are vaporized. The vapors may flow through a coil, where they condense back to liquid, which is then collected in a receiving vessel. In expression, the raw plant material is expressed mechanically or cold-pressed. Expression can be a suitable method where the raw material is available in relatively large quantities at relatively lower cost, such as orange peels for producing citrus-fruit oils. In solvent extraction, a solvent such as hexane or supercritical carbon dioxide is used to extract the oils. Solvent extraction can be a suitable method where the raw material is available in relatively small quantities at relatively higher cost, such as flowers. Solvent extraction can also be a suitable method where the chemical components are too delicate and easily denatured by the high heat used in steam distillation.

A non-exhaustive list of plant species from which essential oils can be extracted to provide a terpenoid in the method 10 of FIG. 1 include: Abies Alba, Abies Balsamea, Abies Sibirica, Achillea Millefolium, Achillea Millefolium Ligustica, Acorus Calamus, Agathophyllum Anisata, Agathophyllum Aromatica, Agathosma Betulina, Agathosma Crenulata, Allium Cepa, Allium Sativum, Aloysia Triphylla, Alpinia Galanga (L.) Sw., Alutinosum Druce, Ammi Visnaga, Amyris Balsamifera, Anethum Graveolens, Angelica Archangelica, Angelica Glauca, Aniba Rosaeodora Var. Amazonica, Anthemis Nobilis, Anthopogon Rhododendron D. Don, Apium Graveolens, Aquilaria Malaccensis, Artemisia Absinthium, Artemisia Afra, Artemisia Annua, Artemisia Dracunculus, Artemisia Pallens, Artemisia Vulgaris, Backhousia Citriodora, Boswellia Carteri, Boswellia Carterii, Boswellia Neglecta, Boswellia Serrata, Bulnesia Sarmienti, Callitris Intratropica, Cananga Odorata, Cananga Odorata Genuina, Cananga Odorata Macrophylla, Canarium Luzonicum, Carum Carvi, Cedrelopsis Grevei, Cedrus Atlantica, Cedrus Deodara, Chamaecyparis Callitropsis Nootkatensis, Chamaecyparis Lawsoniana, Chamaecyparis Obtusa Endl., Chamaemelum Nobile (Anthemis Nobilis), Cinnamomum Camphora, Cinnamomum Camphora L, Cinnamomum Cassia, Cinnamomum Glaucescens, Cinnamomum Polyandrum, Cinnamomum Zeylanicum, Cinnamosma Fragrans, Cistus Ladaniferus, Citrus Aurantifolia, Citrus Aurantium, Citrus Aurantium Var. Amara, Citrus Bergamia, Citrus Bergamia Risso, Citrus Clementine, Citrus Hystrix, Citrus Junos, Citrus Junos Siebold, Citrus Limonum, Citrus Paradisi, Citrus Reticulata, Citrus Sinensis, Citrus Tangerina, Coleonema Album, Commiphora Holtziana, Commiphora Myrrha, Copaifera Officinalis, Coriandrum Sativum, Cotinus Coggygria, Croton Eluteria, Cryptocarya Massoia, Cuminum Cyminum, Cupressus Rotundus, Cupressus Sempervirens, Curcuma Longa, Cymbopogon Citratus, Cymbopogon Flexuosus, Cymbopogon Flexuosus Stapf, Cymbopogon Martini Var. Martinii (Var. Motia), Cymbopogon Nardus, Cymbopogon Winterianus Jewitt, Cymbopogon Winterianus Jowitt, Cympobogan Martini Type Sofia, Cyperus Scariosus, Daucus Carota, Elettaria Cardamomum Maton, Eremophila Mitchellii, Eriocephalus Africanus, Eriocephalus Punctulatus, Eucalyptus Citriodora, Eucalyptus Citriodora Hook., Eucalyptus Dives, Eucalyptus Globulus, Eucalyptus Polybractea, Eucalyptus Radiata, Eucalyptus Smithii, Eugenia Caryophyllata, Ferula Galbaniflua, Foeniculum Vulgare Mill Var Dulce, Foeniculum Vulgare Mill., Fokienia Hodginsil, Gaultheria Procumbens, Geranium Macrorrhizum, Helichrysum Gymnocephalum, Helichrysum Italicum, Helichrysum Stoechas, Hippophae Rhamnoides, Humulus Lupulus, Hydicum Spicatum, Hypericum Perforatum L, Hyssopus Officinalis, Illicium Verum, Juniperus Communis, Juniperus Communis L., Juniperus Oxycedrus, Juniperus Virginiana, Kaempferia Galanga L, Kunzea Ericoides, Lantana Camera, Laurus Nobilis, Lavandula Hybrida, Lavandula Latifolia, Lavandula Officinalis, Leptospermum Petersonii, Leptospermum Scoparium, Levisticum Officinalis, Lippia Citriodora, Lippia Javanica, Litsea Cubeba, Marjorana Hortensis, Matricaria Chamomilla, Matricaria Recutita, Matricaria Recutita, Melaleuca Alternifolia, Melaleuca Minor, Melaleuca Quinquenervia, Melaleuca Viridiflora, Melissa Officinalis, Mentha Arvensis, Mentha Citrata, Mentha Piperita, Mentha Pulegium, Mentha Spicata, Michelia Alba, Mix Of 4 Species, Monarda Fistulosa L., Murraya Koenigii, Myristica Fragrans, Myrocarpus Fastigiatus, Myroxylon Pereirae, Myrtus Communis, Myrtus Communis, Nardostachys Grandiflora, Nardostachys Jatamansi, Nepeta Cataria, Ocimum Basilicum, Ocimum Basilicum L., Ocimum Basillicum, Ocimum Sanctum, Ocotea Cymbarum, Oleum Abies Sibirica, Oleum Chamomille, Oleum Pinus Nigra, Oreganum Vulgare, Origanum Compactum Benth., Origanum Minutiflorum, Origanum Syriacum, Origanum Vulgare, Ormenis Mixta, Pandanus Odoratissimus, Pelargonium Graveolens, Pelargonium×Asperum, Perilla Frutescens Crispa, Petroselinum Crispum, Petroselinum Sativum, Picea Mariana, Pimenta Dioica (Pimenta Officinalis), Pimenta Officinalis, Pimenta Racemosa, Pimpinella Anisum, Pimpinella Anisum L., Pinus Pinaster, Pinus Pumilio, Pinus Sylvestris, Piper Cubeba, Piper Nigrum, Pistacia Lentiscus, Pogostemon Cablin, Prunus Amygdalus, Pseudotsuga Menziesii (Mirb.) Franco, Psiadia Altissima, Rhus Tarantana, Rosmarinus Officinalis, Ruta Graveolens, Salvia Lavandulifolia, Salvia Officinalis, Salvia Sclarea, Salvia Stenophylla, Santalum Album, Santalum Spicatum, Santolina Chamaecyparissus, Satureja Hortensis, Satureja Montana, Schinus Molle, Tagetes Bipinata L, Tagetes Minuta, Tanacetum Annuum Linnaeus, Tarchonanthus Camphoratus, Thuja Occidentalis, Thuja Orientalis, Thuja Plicata, Thujopsis Dolabrata, Thymbra Spicata, Thymus Capitatus, Thymus Mastichina, Thymus Satureioides, Thymus Serpillum, Thymus Vulgare, Thymus Vulgaris, Thymus Zygis, Trachyspermum Ammi, Tsuga Canadensi, Valeriana Officinalis, Vetivera Zizanioides, Vitex Agnus-Castus L, Vitis Vinifera, Xanthoxylum Armatum, Zanthoxylum Armatum Dc. (Rutaceae), Zingiber Cassumunar, Zingiber Officinale, and Zinziber Officinale, among others.

In some embodiments, examples of the essential oil mixture includes mixtures that comprise at least one essential oil extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, Citrus Limonum or a combination thereof. In some embodiments, the essential oil mixture consists essentially of Salvia Sclarea and Pimenta Racemosa. In some of other embodiments, the essential oil mixture consists essentially of Salvia Sclarea and Pistacia Lentiscus. In yet other embodiments, the essential oil mixture consists essentially of Pistacia Lentiscus and Citrus Limonum.

In some other embodiments, the essential oil mixture comprises first and second essential oils extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, or Citrus Limonum, wherein a volume ratio between first and second essential oils is between about 0.01:1 and about 1:1. In some other embodiments, the volume ratio is between about 0.10:1 and about 1:1, or between about 0.50:1 and about 1:1, for instance about 1:1.

Still referring to FIG. 1 , the illustrated method 10 further includes providing one or more mercaptans or one or more flavonoids, or combinations thereof, as described herein (step 35). Representative examples of one or more mercaptans that can be used in accordance with the present invention include but are not limited to mercaptans that are selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan and combinations thereof.

Still referring to FIG. 1 , the illustrated method 10 of preparing an herbal smoking blend further includes adding the terpenoid solution and the one or more mercaptans or one or more flavonoids to the smoking herb preparation (step 40, as shown in FIG. 1 ). The terpenoid solution can be added using a suitable method for incorporating at least a portion of the terpenoid in the terpenoid solution into the smoking herb preparation. The one or more mercaptans or one or more flavonoids can also be added using a suitable method, for example, in liquid form after dilution in a solvent.

In some embodiments, adding the terpenoid solution comprises dropping the terpenoid solution on the smoking herb. As used herein, adding the terpenoid solution by dropping refers to delivering a volume of liquid using, for example, a dropper, to deliver the liquid. In some embodiments, the dropper may deliver the liquid in an amount of between about 5-100 drops per mL, depending on, among other things, the viscosity of the terpenoid solution and the type of dropper used.

In other embodiments, adding the terpenoid solution comprises spraying a mist (or droplets) of the terpenoid solution on the smoking herb. As used herein, adding the terpenoid solution by spraying refers to delivering fine drops of the terpenoid solution dispersed in a gas by using, for example, a spray nozzle or atomizer, to deliver the terpenoid solution. The spray characteristics, including the spray pattern, the spray capacity, and the spray drop size depend on, among other things, the viscosity of the terpenoid solution and the type of spray nozzle used. In yet other embodiments, adding the terpenoid solution comprises spraying using an aerosol spray which includes the terpenoid solution.

In some embodiments, adding the terpenoid solution comprises dipping, or at least partially immersing the smoking herb into the terpenoid solution. By way of an example, the smoking herb can be placed in a dip net or a similar device and lowered into a container containing the terpenoid solution. In some embodiments, a soaking time can be tailored to control the amount of terpenoid solution that is absorbed, impregnated, or incorporated into the smoking herb. In some embodiments, the soaking time is between about 1 second and about 1 day, or between about 10 seconds and about 1 hour, or between about 1 minute and about 10 minutes. The smoking herb can be subsequently dried in air, or by heating the smoking herb, for example at a temperature below a temperature at which the smoking herb ignites.

In some other embodiments, the smoking herb preparation comprises a smoking herb and a rolling paper. In these embodiments, adding the terpenoid solution comprises adding the terpenoid solution to the rolling paper, which can subsequently be used to roll the smoking herb. The terpenoid can be added to the rolling paper using a suitable method to impregnate the rolling paper with the terpenoid solution. For example, the rolling paper can be dipped in a bath of terpenoid solution. Other methods include dropping or spraying the terpenoid solution on the rolling paper. For example, in some embodiments, the terpenoid can be added to a pre-rolled cigarette containing smoking herbs.

It will also be appreciated that the terpenoid solution can be added to the smoking herb by more than one method, for example, by two or more of the methods disclosed herein. For example, the terpenoid solution can be added to the smoking herb by dipping and drying the smoking herb preparation, and subsequently by providing drops of the terpenoid solution to the smoking herb or rolling paper for the smoking herb. In some embodiments, this can increase the concentrations of terpenoids (e.g., volatile terpenoids) in the preparation. In some other embodiments, different terpenoids solutions are added to the smoking herb preparation at different times. For example, a solution with relatively less volatile terpenoids may be added to the smoking herb concentration initially (e.g., hours before consumption, or from a manufacturer or supplier) and a solution with relatively more volatile terpenoids may be added to the smoking herb preparation immediately (e.g., minutes) before smoking.

In some embodiments where the smoking herb preparation includes cannabis, the amount of terpenoid added to the smoking herb preparation exceeds the amount of cannabis terpenoid that was present in the smoking herb prior to adding the terpenoid solution to the smoking herb preparation. In some embodiments, the amount of terpenoid added to the smoking herb preparation exceeds the amount of cannabis terpenoid that was present in the smoking herb prior to adding the terpenoid solution to the smoking herb preparation, such that the overall amount of terpenoid increases by more than about 50%, by about 100%, or by about 1000%.

In some embodiments, the amount of added terpenoid exceeds about 0.001% by weight of the smoking blend, about 0.01% by weight of the smoking blend, or about 0.05% by weight.

In some embodiments, the method 10 of preparing an herbal smoking blend further comprises subjecting the smoking herb preparation to a drying process after adding the terpenoid solution.

FIG. 2 is a schematic illustration of a smoking herb preparation system according to some embodiments. The smoking herb preparation system comprises a smoking herb 80 and a terpenoid and mercaptan or flavonoid solution application kit 70. As described herein, it is to be understood that, in referred embodiments, the terpenoid solution is mixed with one or more mercaptans or one or more flavonoids.

In some embodiments, the terpenoid and mercaptan or flavonoid solution application kit 70 comprises the following:

-   -   (i) a terpenoid solution and one or more mercaptans or one or         more flavonoids (just for illustration purposes only, the         terpenoid solution and one or more mercaptans or one or more         flavonoids mixed together in liquid form are schematically         represented as a combined or mixed liquid 62 in FIG. 2 );     -   (ii) a container 74 for holding the combined or mixed liquid 62         of the terpenoid solution and one or more mercaptans or one or         more flavonoids as described herein; and     -   (iii) an applicator 72 for administering a dose of the combined         or mixed liquid 62 to the smoking herb.

In certain embodiments, the application kit 70 comprises a combined or mixed liquid 62 (just for illustration purposes only, the terpenoid solution and one or more mercaptans or one or more flavonoids together are schematically represented as a combined or mixed liquid 62 in the figures), a container 74 for holding the liquid 62, and an applicator 72 for administering a dose of the combined or mixed liquid 62 to the smoking herb.

Still referring to FIG. 2 , in some embodiments, the combined or mixed liquid 62 can be prepared by using a terpenoid solution preparation system 50. The terpenoid preparation system includes a terpenoid measurement device 52, a terpenoid mixture 54 comprising at least one terpenoid, a solvent measurement device 56, a solvent 58, and a terpenoid solution mixing container 60. The terpenoid measurement device 52 can be any suitable container for measuring and mixing terpenoids to form the terpenoid mixture 54, such as a beaker, a graduated cylinder, a measuring cup, and the like.

At any appropriate or desired time, any one or more of the thiols or mercaptans or one or more flavonoids as described herein (i.e., in liquid form), or any combination thereof, can be added to the terpenoid mixture 54 in any desired or suitable amount or concentration.

In some embodiments, the terpenoid mixture 54 includes one or more terpenoids, such as terpenoids selected from the group consisting of d-limonene, α-pinene, β-myrcene, linalool, pulegone, 1,8-cineole (eucalyptol), α-terpineol, terpineol-4-ol, p-cymene, borneol, Δ-3-carene, β-caryophyllene, caryophyllene oxide, nerolidol, phytol, and combinations thereof. In some other embodiments, the terpenoid mixture 54 includes an essential oil mixture extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, Citrus Limonum, and combinations thereof. The solvent measurement device 56 can be any suitable container for measuring and mixing different solvent components to form the solvent 58, such as a beaker, a graduated cylinder, a measuring cup, and the like. The solvent 58 can include any liquid, e.g., a volatile liquid, which can incorporate a desired amount of the terpenoid in the terpenoid solution. In some embodiments, the solvent components include ethanol and water, in proportions described above.

In some embodiments, the terpenoid solution is formed by mixing the terpenoid mixture 54 and the solvent 58 in the terpenoid solution mixing container 60. The liquid 62 includes the terpenoid mixture 54 incorporated into the solvent 58. As described elsewhere herein, at any appropriate or desired time, any one or more of the thiols or mercaptans or one or more flavonoids as described herein (i.e., in liquid form), or any combination thereof, can be added to the terpenoid mixture 54 in any desired or suitable amount or concentration.

In some embodiments, at least a portion of the terpenoid mixture 54 is miscible in the solvent 58 and can be dissolved in the solvent 58 to form the liquid 62. In other embodiments, at least a portion of the terpenoid mixture 54 is immiscible in the solvent 58 and can be suspended in the solvent 58 to form the liquid 62. As described elsewhere herein, at any appropriate or desired time in the method or process, any one or more of the thiols or mercaptans or one or more flavonoids as described herein (i.e., in liquid form), or any combination thereof, can be added to the terpenoid mixture 54 in any desired or suitable amount or concentration. Just for illustration purposes, the terpenoid solution and one or more mercaptans or one or more flavonoids together are also schematically represented as a combined or mixed liquid by reference numeral 62 in the figures. The liquid 62 can then be transferred into the container 74 of the application kit 70.

Still referring to FIG. 2 , the application kit 70 comprises any suitable applicator 72 for administering a dose of the terpenoid solution and one or more mercaptans or one or more flavonoids, and combinations thereof (again, just for illustration purposes only, the terpenoid solution and one or more mercaptans or one or more flavonoids together are schematically represented as a combined or mixed liquid by reference numeral 62 in the figures), to the smoking herb 80. In some embodiments, the applicator comprises a dropper having a bulb member and a pipette member. The dropper can have any suitable design for forming suitable drops as discussed above for application on the smoking herb 80. For example, the dropper member may have a bulb made of elastic material configured to fill the pipette member with the liquid 62 through a vacuum suction effect. In some embodiments, the dropper may have a threaded closure to enable long term storage of the terpenoid solution. In some embodiments, the pipette member can be graduated to guide a user to administer a predetermined dose of the terpenoid solution on the smoking herb 80. In some other embodiments, the applicator 72 may deliver a stream of the terpenoid solution and one or more mercaptans or one or more flavonoids, and combinations thereof (shown schematically as the combined or mixed liquid 62) to the smoking herb 80, rather than delivering drops. In some other embodiments, the dropper may be integrated into the container 74 itself, which may provide drops directly from an opening in the container 74. For example, the container 74 may be a dropper bottle and the dropper section may be the drop generating opening of the bottle.

FIG. 3 is a schematic illustration of a smoking herb preparation system comprising a smoking herb according to some embodiments. The smoking herb preparation system comprises a smoking herb 80 and an application kit 90. The smoking herb preparation system of FIG. 3 is similar to the smoking herb preparation system of FIG. 2 except for the application kit 90. The terpenoid solution application kit 90 comprises a combined or mixed liquid 62 (as described herein), a container for holding the liquid 62, and an applicator for administering a dose of the combined or mixed liquid 62 to the smoking herb. The container can be, for example, a plastic spray bottle made of plastic, or other reservoir in fluid communication with a nozzle for dispensing the combined or mixed liquid 62, such as an atomizer that dispenses the liquid 62 as mist or spray. The liquid 62 can be mixed in the container and dispensed, for example through an applicator, which can be a trigger sprayer, mounted on the container. In some embodiments, the trigger sprayer may have a threaded closure to enable long term storage of the terpenoid solution. In some embodiments, the trigger sprayer can be configured to administer a predetermined dose of the liquid 62 on the smoking herb 80. The trigger sprayer can also be configured to determine other spray characteristics such as droplet volume, spray angle, etc.

FIG. 4 is a schematic illustration of a smoking herb preparation system comprising a smoking herb according to some embodiments. The smoking herb preparation system comprises a smoking herb 80 and an application kit 90 to administer a predetermined dose of the combined or mixed liquid 62. While the smoking herb preparation system of FIG. 4 includes application kit 90 that is similar to FIG. 3 , an application kit similar to the application kit 70 of FIG. 2 , or any other similar application kits can be used. In addition, the smoking herb preparation system of FIG. 4 further includes a rolling sheet 104. The smoking herb preparation system of FIG. 4 is configured such that the combined or mixed liquid 62 can be incorporated into the rolling sheet 104 instead of, or in addition to, incorporating the combined or mixed liquid 62 into the smoking herb 80 using the application kit 90. In these embodiments, the resulting rolling sheet 104 can be subsequently dried and used to roll the smoking herb 80 into a thin cylinder 110 having the smoking herb 80 rolled therein, in a similar manner to a rolled cigarette. In some embodiments, the rolling sheet 104 can be a paper made from wood pulp. In other embodiments, the rolling sheet 104 can be made from rice or other plant matter such as hemp. In some other embodiments, the rolling sheet 104 can be a pre-formed wrapper (e.g., a cylindrical wrapper) for holding smoking herb 80.

Although this invention has been described in terms of certain non-limiting embodiments, other embodiments are also within the scope of this invention. Moreover, the various embodiments described above can be combined to provide further embodiments. In addition, certain features shown in the context of one embodiment can be incorporated into other embodiments as well. 

1. A method of preparing an herbal smoking blend, comprising: providing a smoking herb preparation comprising cannabis; providing a terpenoid solution comprising at least one terpenoid; providing one or more mercaptans or one or more flavonoids; and adding the terpenoid solution and adding the one or more mercaptans or the one or more flavonoids to the smoking herb preparation.
 2. The method of claim 1, wherein the terpenoid is not naturally occurring in the herb preparation.
 3. The method of claim 1, wherein the terpenoid is selected from the group consisting of pulegone, terpineol-4-ol, p-cymene, borneol, eugenol, sabinene, linalyl acetate, chamazulene, beta-farnesene, benzyl benzoate, benzyl acetate, geraniol, geranyl acetate and combinations thereof.
 4. The method of claim 1, wherein the terpenoid solution comprises an essential oil mixture.
 5. The method of claim 4, wherein the essential oil mixture comprises at least one essential oil extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, Citrus Limonum or a combination thereof.
 6. The method of claim 4, wherein the essential oil mixture comprises first and second essential oils extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, or Citrus Limonum, and wherein a volume ratio between first and second essential oils is between about 0.01:1 and about 1:1.
 7. The method of claim 4, wherein the terpenoid solution further comprises a solvent, wherein the solvent comprises ethanol and water.
 8. The method of claim 4, wherein the terpenoid solution comprises about 1% to about 5% by volume of the essential oil mixture, about 40% to about 90% by volume of ethanol and about 10% to about 30% by volume of water.
 9. The method of claim 1, wherein the smoking herb preparation comprises any type of cannabinoid or any combination of cannabinoids.
 10. The method of claim 1, wherein the smoking herb preparation comprises at least one phytocannabinoid selected from the group consisting of delta-9-tetrahydrocannabinol (THC), cannabidiol (CBD), cannabichromene (CBC), cannabigerol (CBG), tetrandrocannabivarin (THCV), cannabidivarin (SBDV) and cannabinol (CBN).
 11. The method of claim 10, wherein the smoking herb preparation comprises a smoking herb other than cannabis.
 12. The method of claim 1, wherein the terpenoid is derived from a plant other than cannabis.
 13. The method of claim 1, wherein adding the terpenoid solution comprises applying the terpenoid solution in a liquid state to the smoking herb preparation, and adding the one or more mercaptans comprises applying the one or more mercaptans in a liquid state to the smoking herb preparation.
 14. The method of claim 13, wherein adding the terpenoid solution comprises dropping droplets of the terpenoid solution onto the smoking herb preparation, and adding the one or more mercaptans comprises dropping droplets of the one or more mercaptans onto the smoking herb preparation.
 15. The method of claim 13, wherein adding the terpenoid solution comprises at least partially immersing the smoking herb into the terpenoid solution.
 16. The method of claim 1, wherein the smoking herb preparation comprises a smoking herb rolled in a rolling paper, and wherein adding the terpenoid comprises impregnating the rolling paper with the terpenoid solution.
 17. The method of claim 1, wherein the smoking herb preparation comprises a smoking herb and a rolling sheet, and wherein the method further comprises rolling the smoking herb into a cylinder to at least partially confine the smoking herb.
 18. The method of claim 1, wherein an amount of the at least one terpenoid added to the smoking herb preparation exceeds a naturally existing amount of cannabis terpenoid in the smoking herb by about 10% to about 1000%.
 19. The method of claim 1, wherein the one or more mercaptans are selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan and combinations thereof.
 20. A smoking herb preparation system, comprising: a smoking herb comprising cannabis; a terpenoid solution comprising at least one terpenoid; one or more mercaptans; and an applicator for administering a dose of the terpenoid solution and the one or more mercaptans, and combinations thereof, to the smoking herb.
 21. The system of claim 20, wherein the terpenoid is not naturally occurring in the herb preparation.
 22. The system of claim 20, wherein the at least one terpenoid selected from the group consisting of pulegone, terpineol-4-ol, p-cymene, borneol, eugenol, sabinene, linalyl acetate, chamazulene, beta-farnesene, benzyl benzoate, benzyl acetate, geraniol, geranyl acetate and combinations thereof.
 23. The system of claim 20, wherein the terpenoid solution comprises an essential oil mixture.
 24. The system of claim 23, wherein the essential oil mixture comprises at least one essential oil extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, Citrus Limonum, and combinations thereof.
 25. The system of claim 20, wherein the terpenoid solution further comprises a solvent including ethanol and water.
 26. The system of claim 20, wherein the applicator comprises a dropper.
 27. The system of claim 20, wherein the applicator comprises a sprayer.
 28. The system of claim 20, wherein the one or more mercaptans are selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan and combinations thereof.
 29. An herbal smoking blend, comprising: a smoking herb comprising cannabis; a terpenoid incorporated in the smoking herb at a terpenoid concentration, wherein the terpenoid is not naturally occurring in the smoking herb at the terpenoid concentration; and one or more mercaptans.
 30. The herbal smoking blend of claim 29, wherein the herbal smoking blend comprises at least one essential oil extracted from the group of plants consisting of Salvia Sclarea, Pimenta Racemosa, Pistacia Lentiscus, Citrus Limonum, and combinations thereof.
 31. The herbal smoking blend of claim 29, wherein the terpenoid is not naturally occurring in the smoking herb.
 32. The herbal smoking blend of claim 29, wherein the terpenoid is selected from the group consisting of pulegone, terpineol-4-ol, p-cymene, borneol, eugenol, sabinene, linalyl acetate, chamazulene, beta-farnesene, benzyl benzoate, benzyl acetate, geraniol, geranyl acetate and combinations thereof.
 33. The herbal smoking blend of claim 29, wherein the one or more mercaptans are selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan and combinations thereof.
 34. A smoking herb preparation system, comprising: a smoking herb comprising cannabis; a terpenoid solution comprising a terpenoid selected from the group consisting of 1,8-cineole, d-limonene, α-terpineol and combinations thereof; one or more mercaptans selected from the group consisting of allyl mercaptan, amyl mercaptan, isoamyl mercaptan, sec-amyl mercaptan, tert-amyl mercaptan, benzyl mercaptan, buchu mercaptan, butyl mercaptan, isobutyl mercaptan, tert-butyl mercaptan, cyclohexyl mercaptan, cyclopentyl mercaptan, 2-ethyl hexyl mercaptan, ethyl mercaptan, ethylene mercaptan, furfuryl mercaptan, grapefruit mercaptan, heptyl mercaptan, hexyl mercaptan, methyl mercaptan, 2-naphthyl mercaptan, octyl mercaptan, peach mercaptan, 1-phenethyl mercaptan, 2-phenethyl mercaptan, phenyl mercaptan, prenyl mercaptan, propyl mercaptan, isopropyl mercaptan, 2-thienyl mercaptan, 3-thienyl mercaptan and combinations thereof; and an applicator for administering a dose of the terpenoid solution and the one or more mercaptans, and combinations thereof, to the smoking herb.
 35. A method of preparing an herbal smoking blend, comprising: providing a smoking herb preparation comprising cannabis; providing a terpenoid solution comprising at least one terpenoid; providing one or more mercaptans; providing one or more flavonoids; and adding the terpenoid solution, adding the one or more mercaptans, and adding the one or more flavonoids to the smoking herb preparation.
 36. An herbal smoking blend, comprising: a smoking herb comprising cannabis; a terpenoid incorporated in the smoking herb at a terpenoid concentration, wherein the terpenoid is not naturally occurring in the smoking herb at the terpenoid concentration; one or more mercaptans; and one or more flavonoids. 